Cisema is a leading provider of regulatory affairs, quality compliance, clinical research, and product testing & safety certification for China, Hong Kong, South Korea, Taiwan and Southeast Asia (Malaysia, Singapore, Vietnam, Indonesia, Thailand and the Philippines).
We enable compliance for across various industry sectors including medical devices, in-vitro diagnostics (IVD), pharmaceuticals, veterinary drugs, pet food, cosmetics, health supplements, machinery and consumer goods. Whether providing regulatory advice on market entry strategies, acting as your local authorized representative, registering your products, achieving customs clearance, adapting your QMS, or preparing you for factory inspections, Cisema offers comprehensive regulatory and quality compliance services.
Founded in 2002, we have expanded to many offices globally over the last 20+ years, with service delivery operations in Asia Pacific and sales representative offices worldwide. Our expertise covers product approvals of all classes, therapeutic areas, types and specifications, benefitting startups, SMEs or MNCs alike.
Professional Services
Additional Information
Other Place of Business
Year of Establishment
2002
Service Introduction
Terms and Conditions & Disclaimer
I agreeAt which key stages of the project lifecycle are your services appropriately applied?
Vice President
Cisema
Service
Regulatory Affairs & Market Access Solutions for Greater China and Asia
Regulatory affairs and market access consultancy helping healthcare companies successfully launch products across Greater China, South Korea, and Southeast Asia.
Vice President at Cisema
China (Hong Kong)